Evidence map›Paper›PMID 21387562›Full record

ArticleEMBO molecular medicine2011

Pml represses tumour progression through inhibition of mTOR.

Rosa Bernardi, Antonella Papa, Ainara Egia, Nadia Coltella, Julie Teruya-Feldstein, Sabina Signoretti, Pier Paolo Pandolfi

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. PML mediates glioblastoma resistance to mammalian target of rapamycin (mTOR)-targeted therapies.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Is PML a Tumor Suppressor?Frontiers in oncology · 2013
    Article
  14. Article
  15. The nuclear bodies inside out: PML conquers the cytoplasm.Current opinion in cell biology · 2011
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Rosa BernardiCancer Genetics Program, Beth Israel Deaconess Cancer Center, Division of Genetics, Department of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. bernardi.rosa@hsr.it
Antonella Papa
Ainara Egia
Nadia Coltella
Julie Teruya-Feldstein
Sabina Signoretti
Pier Paolo Pandolfi
Beth Israel Deaconess Medical Center · USCancer Genetics (United States) · USBrigham and Women's Hospital · USMemorial Sloan Kettering Cancer Center · USSan Raffaele University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The promyelocytic leukaemia gene PML is a pleiotropic tumour suppressor. We have recently demonstrated that PML opposes mTOR-HIF1α-VEGF signalling in hypoxia. To determine the relevance of PML-mTOR antagonism in tumourigenesis, we have intercrossed Pml null mice with Tsc2 heterozygous mice, which develop kidney cysts and carcinomas exhibiting mTOR upregulation. We find that combined inactivation of Pml and Tsc2 results in aberrant TORC1 activity both in pre-tumoural kidneys as well as in kidney lesions. Such increase correlates with a marked acceleration in tumour progression, impacting on both the biology and histology of kidney carcinomas. Also, Pml inactivation decreases the rate of loss of heterozygosity (LOH) for the wt Tsc2 allele. Interestingly, however, aberrant TORC1 activity does not accelerate renal cystogenesis in Tsc2/Pml mutants. Our data demonstrate that activation of mTOR is critical for tumour progression, but not for tumour initiation in the kidney.

Indexed as

Gene Expression RegulationAnimalsCarcinomaCrosses, GeneticHistocytochemistryImmunohistochemistryKidneyKidney NeoplasmsMagnetic Resonance ImagingMiceMice, KnockoutNuclear ProteinsPromyelocytic Leukemia ProteinRadiography, AbdominalRepressor ProteinsTOR Serine-Threonine KinasesCrtc1 protein, mousemTOR protein, mouseNuclear ProteinsPml protein, mousePromyelocytic Leukemia ProteinRepressor ProteinsTOR Serine-Threonine KinasesTranscription FactorsTsc2 protein, mouseTuberous Sclerosis Complex 2 ProteinTumor Suppressor Proteins

Identifiers

PMID21387562
PMCPMC3123467
OpenAlexW2114762733

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.